T.W. POWER SUPPLY VH-3010

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-06-25 for T.W. POWER SUPPLY VH-3010 manufactured by Maquet Cardiovascular Llc.

MAUDE Entry Details

Report Number2242352-2019-00710
MDR Report Key8730959
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-06-25
Date of Report2019-06-21
Date of Event2019-06-03
Date Mfgr Received2019-08-14
Device Manufacturer Date2017-04-03
Date Added to Maude2019-06-25
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer Street45 BARBOUR POND DRIVE
Manufacturer CityWAYNE NJ 07470
Manufacturer CountryUS
Manufacturer Postal07470
Manufacturer G1MAQUET CARDIOVASCULAR LLC
Manufacturer Street45 BARBOUR POND DRIVE
Manufacturer CityWAYNE NJ 07470
Manufacturer CountryUS
Manufacturer Postal Code07470
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameT.W. POWER SUPPLY
Generic NameUNIT, CAUTERY, THERMAL, AC-POWERED
Product CodeHQO
Date Received2019-06-25
Catalog NumberVH-3010
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMAQUET CARDIOVASCULAR LLC
Manufacturer Address45 BARBOUR POND DRIVE WAYNE NJ 07470 US 07470


Patients

Patient NumberTreatmentOutcomeDate
10 2019-06-25

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